Canonical Allele Identifier: CA1940191030
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669995C= , CM000672.2:g.119669995C= GRCh38
NC_000010.10:g.121429507C= , CM000672.1:g.121429507C= GRCh37
NC_000010.9:g.121419497C= NCBI36
NG_016125.1:g.23626C= , LRG_742:g.23626C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.325C= MANE Select ENSP00000358081.4:p.His109=
ENST00000369085.7:c.325C= ENSP00000358081.3:p.His109=
ENST00000450186.1:c.151C= ENSP00000410036.1:p.His51=
NM_004281.3:c.325C= , LRG_742t1:c.325C= NP_004272.2:p.His109=
XM_005270287.1:c.325C= XP_005270344.1:p.His109=
XM_005270287.2:c.325C= XP_005270344.1:p.His109=
NM_004281.4:c.325C= MANE Select NP_004272.2:p.His109=